1,131 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LOGIQ
FDA UDI
GE Medical Systems (China) Co.,Ltd.·00195278674197·LOGIQ e TP Standard Console
ETEST® Ertapenem (ETP)
FDA UDI
BIOMERIEUX SA·03573026550486·Etest is a quantitative technique for determini...
ETEST® Ertapenem (ETP)
FDA UDI
BIOMERIEUX SA·03573026547226·Etest is a quantitative technique for determini...
ETEST® Ertapenem (ETP)
FDA UDI
BIOMERIEUX SA·03573026619923·ETEST® is a manual, quantitative technique for ...
ETP 180 CARDIAC PACEMAKER (EXTERNAL)
FDA 510(k)
FDA Class 2
·Cardiovascular
Sharn Inc
FDA UDI
Sharn Anesthesia·00817518021430·FLEX-TIP ET TUBES, LOW PROFILE 9.5 10/PK
Sharn Inc
FDA UDI
Sharn Anesthesia·00817518021423·FLEX-TIP ET TUBES, HIGH VOLUME /LOW PRESS SIZE ...
Sharn Inc
FDA UDI
Sharn Anesthesia·00817518021447·FLEX-TIP REINFORCED ENDO TUBES CUFFED 9.5 10/PK
ETP 180A NON-INVASIVE EXTERNAL PACEMAKER
FDA 510(k)
FDA Class 2
·Cardiovascular
ETP 300 NON-INVASIVE EXTERNAL PACEMAKER
FDA 510(k)
FDA Class 2
·Cardiovascular
ETP 180E NON-INVASIVE EXTERNAL PACEMAKER
FDA 510(k)
FDA Class 2
·Cardiovascular
VITEK 2 GRAM-NEGATIVE SUSCEPTIBILITY TEST KIT AST-N233
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, INC.·Product code LON·June 11, 2015
VITEK® 2 AST-GN70 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·July 30, 2018
ETEST® ERTAPENEM ETP 32 WW B30
FDA Adverse Event
Malfunction
·BIOMERIEUX, SA·Product code JWY·March 29, 2017
BD PHOENIX PANEL NMIC-306
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 12, 2022
ETEST® ERTAPENEM ETP 32 WW B30
FDA Adverse Event
Malfunction
·BIOMERIEUX, SA·Product code JWY·February 23, 2017
BD PHOENIX PANEL NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 14, 2024
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 26, 2025
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 26, 2025
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 26, 2025